NOP14 suppresses breast cancer progression by inhibiting NRIP1/Wnt/β-catenin pathway

被引:26
作者
Lei, Jin-Ju [1 ]
Peng, Rou-Jun [2 ]
Kuang, Bo-Hua [1 ]
Yuan, Zhong-Yu [2 ]
Qin, Tao [2 ]
Liu, Wen-Sheng [1 ]
Guo, Yun-Miao [1 ]
Han, Hui-Qiong [1 ]
Lian, Yi-Fan [1 ]
Deng, Cheng-Cheng [1 ]
Zhang, Hao-Jiong [1 ]
Chen, Li-Zhen [1 ]
Feng, Qi-Sheng [1 ]
Xu, Miao [1 ]
Feng, Lin [1 ]
Bei, Jin-Xin [1 ]
Zeng, Yi-Xin [1 ,3 ]
机构
[1] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol South China, Dept Expt Res,Collaborat Innovat Ctr Canc Med, Guangzhou 510275, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol South China, Dept Med Oncol,Collaborat Innovat Ctr Canc Med, Guangzhou 510275, Guangdong, Peoples R China
[3] Peking Union Med Coll, Beijing 100021, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
NOP14; breast cancer; NRIP1; Wnt/beta-catenin pathway; STEM-CELLS; IN-VITRO; METASTASIS; EXPRESSION; BINDING;
D O I
10.18632/oncotarget.4573
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
NOP14, which is functionally conserved among eukaryotes, has been implicated in cancer development. Here, we show that NOP14 is poorly expressed in breast cancer cells and invasive breast cancer tissues. In vivo and in vitro studies indicated that NOP14 suppressed the tumorigenesis and metastasis of breast cancer cells. Further investigations revealed that NOP14 enhanced ER alpha expression and inhibited the Wnt/beta-catenin pathway by up-regulating NRIP1 expression. Survival analysis indicated that low NOP14 expression was significantly associated with poor overall survival (P = 0.0006) and disease-free survival (P = 0.0007), suggesting that NOP14 is a potential prognostic factor in breast cancer. Taken together, our findings reveal that NOP14 may suppress breast cancer progression and provide new insights into the development of targeted therapeutic agents for breast cancer.
引用
收藏
页码:25701 / 25714
页数:14
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